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Species-Conserved SYNGAP1 Phenotypes Associated with Neurodevelopmental Disorders
SYNGAP1 loss-of-function variants are causally associated with intellectual disability, severe epilepsy, autism spectrum disorder and schizophrenia. While there are hundreds of genetic risk factors for neurodevelopmental disorders (NDDs), this gene is somewhat unique because of the frequency and pen...
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| Publicado no: | Mol Cell Neurosci |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6128754/ https://ncbi.nlm.nih.gov/pubmed/29580901 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mcn.2018.03.008 |
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